Method of stimulating an immune response with activated dendritic cells

ABSTRACT

Antigen-expressing, activated dendritic cells are disclosed. Such dendritic cells are used to present tumor, viral or bacterial antigens to T cells, and can be useful in vaccination protocols. Other cytokines can be used in separate, sequential or simultaneous combination with the activated, antigen-pulsed dendritic cells. Also disclosed are methods for stimulating an immune response using the antigen-expressing, activated dendritic cells.

This application is a continuation of application Ser. No. 08/763,995,filed Dec. 12, 1996, now U.S. Pat. No. 6,017,527, which is a CON ofapplication Ser. No. 08/677,762, filed Jul. 10, 1996, now abandoned.

FIELD OF THE INVENTION

The present invention relates to a dendritic cell activation factor, tomethods of enhancing a lymphocyte-mediated immune response in vivo, andto dendritic cell populations useful in the manipulation of cellular andhumoral immune responses.

BACKGROUND OF THE INVENTION

Vaccination is an efficient means of preventing death or disability frominfectious diseases. The success of this method in the field ofinfectious disease has also stimulated interest in utilizing vaccinationin the treatment or prevention of neoplastic disease. Despite thesuccesses achieved with the use of vaccines, however, there are stillmany challenges in the field of vaccine development. Parenteral routesof administration, the numbers of different vaccinations required andthe need for, and frequency of, booster immunizations all impede effortsto control or eliminate disease.

One such difficulty is lack of immunogenicity in an antigen, i.e., theantigen is unable to promote an effective immune response against thepathogen. In addition, certain antigens may elicit only a certain typeof immune response, for example, a cell-mediated or a humoral response.Adjuvants are substances that enhance, augment or potentiate an immuneresponse, and can in some instances be used to promote one type ofimmune response over another. Although numerous vaccine adjuvants areknown, alum is the only adjuvant widely used in humans.

Dendritic cells are a heterogeneous cell population with distinctivemorphology and a widespread tissue distribution (Steinman, R. M., Annu.Rev. Immunol., 9:271-296, 1991). Dendritic cells are referred to as“professional” antigen presenting cells, and have a high capacity forsensitizing MHC-restricted T cells. Thus, there is growing interest inusing dendritic cells ex vivo as tumor or infectious disease vaccineadjuvants (see, for example, Romani, et al., J. Exp. Med., 180:83,1994). Therefore, an agent that enhanced the ability of dendritic cellsto stimulate an immune response would be of wide importance.

SUMMARY OF THE INVENTION

The present invention pertains to a method of activating dendritic cellsto enhance antigen presenting capacity. The activated,antigen-presenting dendritic cells of the invention are useful asvaccine adjuvants.

The invention also provides a method of generating large quantities ofantigen-presenting dendritic cells ex vivo. Following collection of anindividual's CD34⁺ hematopoietic progenitors and stem cells, cytokinessuch as granulocyte-macrophage colony stimulating factor (GM-CSF) andflt-3 ligand (flt3-L) can be used to expand the cells in vitro and todrive them to differentiate into cells of the dendritic cell lineage.Cytokines can also be used to increase the numbers of CD34⁺ cells incirculation prior to collection. The resulting dendritic cells areexposed to an antigen one wishes to elicit an immune response against,and allowed to process the antigen (this procedure is sometimes referredto in the art as “antigen-pulsing”). The antigen-pulsed (orantigen-expressing) dendritic cells are then activated with a CD40binding protein, and subsequently administered to the individual.

An alternate method for preparing dendritic cells that present antigenis to transfect the dendritic cells with a gene encoding an antigen or aspecific polypeptide derived therefrom. Once the dendritic cells expressthe antigen in the context of MHC, the dendritic cells are activatedwith a CD40 binding protein, and subsequently administered to theindividual to provide a stronger and improved immune response to theantigen.

The activated antigen-presenting dendritic cells can also be used as avaccine adjuvant and can be administered prior to, concurrently with orsubsequent to antigen administration. Moreover, the dendritic cells canbe administered to the individual prior to, concurrently with orsubsequent to administration of cytokines that modulate an immuneresponse, for example a CD40 binding protein (i.e., soluble CD40L), or asoluble CD83 molecule. Additional useful cytokines include, but are notlimited to, Interleukins (IL) 1, 2, 4, 5, 6, 7, 10, 12 and 15, colonystimulating factors (CSF) such as GM-CSF, granulocyte colony stimulatingfactor (G-CSF), or GM-CSF/IL-3 fusion proteins, or other cytokines suchas TNF-α or c-kit ligand. Moreover, biologically active derivatives ofthese cytokines; and combinations thereof will also be useful.

The invention also provides for the ex vivo preparation ofantigen-specific T cells. Following the procedures described above forpreparing large numbers of antigen-presenting dendritic cells ex vivo,the collected antigen-presenting dendritic cells are used to generateantigen-specific T cells from naive T cells that have been collectedfrom the individual. After the antigen has been adequately presented tothe T cells generated, the antigen-specific T cells can be administeredto the individual.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 presents the results of an allo-antigen T cell proliferationassay, demonstrating that incubation of dendritic cells with CD40L priorto their use in an MLR (mixed lymphocyte reaction) increases the abilityof the dendritic cells to stimulate the proliferation of T cells byabout threefold, as described in Example 3.

FIG. 2 illustrates that dendritic cells that are cultured with CD40L areless effective at presenting antigen to antigen-specific T cells thandendritic cells that were not exposed to CD40L, as described in Example4.

FIG. 3 demonstrates that that dendritic cells that are first pulsed withantigen, then cultured with CD40L are more effective at presentingantigen to antigen-specific T cells than dendritic cells that werepulsed with antigen but not exposed to CD40L, as described in Example 5.

DETAILED DESCRIPTION OF THE INVENTION

The invention is directed to the use of CD40L to activate antigen-pulseddendritic cells. Activation enhances the ability of the dendritic cellsto present antigen to lymphoid cells, and thus augments the immuneresponse against the antigen. Another embodiment of the invention is theisolation and use of activated, antigen-pulsed dendritic cells asvaccine adjuvants. The activated, antigen-pulsed dendritic cells mayalso be used ex vivo to generate antigen-specific T cells.

Dendritic Cells

Dendritic cells comprise a heterogeneous cell population withdistinctive morphology and a widespread tissue distribution. Thedendritic cell system and its role in immunity is reviewed by Steinman,R. M., Annu. Rev. Immunol., 9:271-296 (1991), incorporated herein byreference. The cell surface of dendritic cells is unusual, withcharacteristic veil-like projections, and is characterized by having thecell surface markers CD1a⁺, CD4⁺, CD86⁺, or HLA-DR⁺. Dendritic cellshave a high capacity for sensitizing MHC-restricted T cells and are veryeffective at presenting antigens to T cells in situ, both self-antigensduring T cell development and tolerance and foreign antigens duringimmunity.

Because of their effectiveness at antigen presentation, there is growinginterest in using dendritic cells ex vivo as tumor or infectious diseasevaccine adjuvants (see, for example, Romani, et al., J. Exp. Med.,180:83 (1994). The use of dendritic cells as immunostimulatory agentshas been limited due to the low frequency of dendritic cells inperipheral blood, the limited accessibility of lymphoid organs and thedendritic cells' terminal state of differentiation. Dendritic cellsoriginate from CD34+ bone marrow or peripheral blood progenitors andperipheral blood mononuclear cells, and the proliferation and maturationof dendritic cells can be enhanced by the cytokines GM-CSF sargramostim,Leukine®, Immunex Corporation, Seattle, Wash.), TNF-α, c-kit ligand(also known as stem cell factor (SCF), steel factor (SF), or mast cellgrowth factor (MGF)) and interleukin-4. Recently, flt3-L has been foundto stimulate the generation of large numbers of functionally maturedendritic cells, both in vivo and in vitro (U.S. Ser. No. 08/539,142,filed Oct. 4, 1995).

Ex Vivo Culture of Dendritic Cells

A procedure for ex vivo expansion of hematopoietic stem and progenitorcells is described in U.S. Pat. No. 5,199,942, incorporated herein byreference. Other suitable methods are known in the art. Briefly, ex vivoculture and expansion comprises: (1) collecting CD34⁺ hematopoietic stemand progenitor cells from a patient from peripheral blood harvest orbone marrow explants; and (2) expanding such cells ex vivo. In additionto the cellular growth factors described in U.S. Pat. No. 5,199,942,other factors such as flt3-L, IL-1, IL-3 and c-kit ligand, can be used.

Stem or progenitor cells having the CD34 marker constitute only about 1%to 3% of the mononuclear cells in the bone marrow. The amount of CD34⁺stem or progenitor cells in the peripheral blood is approximately 10- to100-fold less than in bone marrow. Cytokines such as flt3-L may be usedto increase or mobilize the numbers of dendritic cells in vivo.Increasing the quantity of an individual's dendritic cells mayfacilitate antigen presentation to T cells for antigen(s) that alreadyexists within the patient, such as a tumor antigen, or a bacterial orviral antigen. Alternatively, cytokines may be administered prior to,concurrently with or subsequent to administration of an antigen to anindividual for immunization purposes.

Peripheral blood cells are collected using apheresis procedures known inthe art. See, for example, Bishop et al., Blood, vol. 83, No. 2, pp.610-616 (1994). Briefly, peripheral blood progenitor cells (PBPC) andperipheral blood stem cells (PBSC) are collected using conventionaldevices, for example, a Haemonetics Model V50 apheresis device(Haemonetics, Braintree, Mass.). Four-hour collections are performedtypically no more than five times weekly until approximately 6.5×108mononuclear cells (MNC)/kg are collected. The cells are suspended instandard media and then centrifuged to remove red blood cells andneutrophils. Cells located at the interface between the two phases (thebuffy coat) are withdrawn and resuspended in HBSS. The suspended cellsare predominantly mononuclear and a substantial portion of the cellmixture are early stem cells.

A variety of cell selection techniques are known for identifying andseparating CD34⁺ hematopoietic stem or progenitor cells from apopulation of cells. For example, monoclonal antibodies (or otherspecific cell binding proteins) can be used to bind to a marker proteinor surface antigen protein found on stem or progenitor cells. Severalsuch markers or cell surface antigens for hematopoietic stem cells(i.e., flt-3, CD34, My-10, and Thy-1) are known in the art, as arespecific binding proteins therefore (see for example, U.S. Ser. No.08/539, 142, filed Oct. 4, 1995).

In one method, antibodies or binding proteins are fixed to a surface,for example, glass beads or flask, magnetic beads, or a suitablechromatography resin, and contacted with the population of cells. Thestem cells are then bound to the bead matrix. Alternatively, the bindingproteins can be incubated with the cell mixture and the resultingcombination contacted with a surface having an affinity for theantibody-cell complex. Undesired cells and cell matter are removedproviding a relatively pure population of stem cells. The specific cellbinding proteins can also be labeled with a fluorescent label, e.g.,chromophore or fluorophore, and the labeled cells separated by sorting.Preferably, isolation is accomplished by an immunoaffinity column.

Immunoaffinity columns can take any form, but usually comprise a packedbed reactor. The packed bed in these bioreactors is preferably made of aporous material having a substantially uniform coating of a substrate.The porous material, which provides a high surface area-to-volume ratio,allows for the cell mixture to flow over a large contact area while notimpeding the flow of cells out of the bed. The substrate should, eitherby its own properties, or by the addition of a chemical moiety, displayhigh-affinity for a moiety found on the cell-binding protein. Typicalsubstrates include avidin and streptavidin, while other conventionalsubstrates can be used.

In one useful method, monoclonal antibodies that recognize a cellsurface antigen on the cells to be separated are typically furthermodified to present a biotin moiety. The affinity of biotin for avidinthereby removably secures the monoclonal antibody to the surface of apacked bed (see Berenson, et al., J. Immunol. Meth., 91:11, 1986). Thepacked bed is washed to remove unbound material, and target cells arereleased using conventional methods. Immunoaffinity columns of the typedescribed above that utilize biotinylated anti-CD34 monoclonalantibodies secured to an avidin-coated packed bed are described forexample, in WO 93/08268.

An alternative means of selecting the quiescent stem cells is to inducecell death in the dividing, more lineage-committed, cell types using anantimetabolite such as 5-fluorouracil (5-FU) or an alkylating, agentsuch as 4-hydroxycyclophosphamide (4-HC). The non-quiescent cells arestimulated to proliferate and differentiate by the addition of growthfactors that have little or no effect on the stem cells, causing thenon-stem cells to proliferate and differentiate and making them morevulnerable to the cytotoxic effects of 5-FU or 4-HC. See Berardi et al.,Science, 267:104 (1995), which is incorporated herein by reference.

Isolated stem cells can be frozen in a controlled rate freezer (e.g.,Cryo-Med, Mt. Clemens, Mich.), then stored in the vapor phase of liquidnitrogen using dimethylsulfoxide as a cryoprotectant. A variety ofgrowth and culture media can be used for the growth and culture ofdendritic cells (fresh or frozen), including serum-depleted orserum-based media. Useful growth media include RPMI, TC 199, Iscovesmodified Dulbecco's medium (Iscove, et al., F. J. Exp. Med., 147:923(1978)), DMEM, Fischer's, alpha medium, NCTC, F-10, Leibovitz's L-15,MEM and McCoy's.

Particular nutrients present in the media include serum albumin,transferrin, lipids, cholesterol, a reducing agent such as2-mercaptoethanol or monothioglycerol, pyruvate, butyrate, and aglucocorticoid such as hydrocortisone 2-hemisuccinate. Moreparticularly, the standard media includes an energy source, vitamins orother cell-supporting organic compounds, a buffer such as HEPES, orTris, that acts to stabilize the pH of the media, and various inorganicsalts. A variety of serum-free cellular growth media is described in WO95/00632, which is incorporated herein by reference.

The collected CD34⁺ cells are cultured with suitable cytokines, forexample, as described herein, and in U.S. Ser. No. 08/539,142. CD34⁺cells then are allowed to differentiate and commit to cells of thedendritic lineage. These cells are then further purified by flowcytometry or similar means, using markers characteristic of dendriticcells, such as CD1a, HLA DR, CD80 and/or CD86. The cultured dendriticcells are exposed to an antigen, for example, a tumor antigen or anantigen derived from a pathogenic or opportunistic organism, allowed toprocess the antigen, and then cultured with an amount of a CD40 bindingprotein to activate the dendritic cell. Alternatively, the dendriticcells are transfected with a gene encoding an antigen, and then culturedwith an amount of a CD40 binding protein to activate theantigen-presenting dendritic cells.

The activated, antigen-carrying dendritic cells are them administered toan individual in order to stimulate an antigen-specific immune response.The dendritic cells can be administered prior to, concurrently with, orsubsequent to, antigen administration. Alternatively, T cells may becollected from the individual and exposed to the activated,antigen-carrying dendritic cells in vitro to stimulate antigen-specificT cells, which are administered to the individual.

Useful Cytokines

Various cytokines will be useful in the ex vivo culture of dendriticcells. Flt3-L refers to a genus of polypeptides that are described in EP0627487 A2 and in WO 94/28391, both incorporated herein by reference. Ahuman flt3-L cDNA was deposited with the American Type CultureCollection, Rockville, Md., USA (ATCC) on Aug. 6, 1993 and assignedaccession number ATCC 69382. IL-3 refers to a genus of interleukin-3polypeptides as described in U.S. Pat. No. 5,108,910, incorporatedherein by reference. A DNA sequence encoding human IL-3 protein suitablefor use in the invention is publicly available from the American TypeCulture Collection (ATCC) under accession number ATCC 67747. c-kitligand is also referred to as Mast Cell Growth Factor (MGF), SteelFactor or Stem Cell Factor (SCF), and is described in EP 423,980, whichis incorporated herein by reference.

Other useful cytokines include Interleukin-4 (IL-4; Mosley et al., Cell59:335 (1989), Idzerda et al., J. Exp. Med. 171:861 (1990) and Galizziet al., Intl. Immunol. 2:669 (1990), each of which is incorporatedherein by reference) and granulocyte-macrophage colony stimulatingfactor (GM-CSF; described in U.S. Pat. Nos. 5,108,910, and 5,229,496each of which is incorporated herein by reference). Commerciallyavailable GM-CSF (sargramostim, Leukine®) is obtainable from ImmunexCorp., Seattle, Wash.). Moreover, GM-CSF/IL-3 fusion proteins (i.e., aC-terminal to N-terminal fusion of GM-CSF and IL-3) will also be usefulin ex vivo culture of dendritic cells. Such fusion proteins are knownand are described in U.S. Pat. Nos. 5,199,942, 5,108,910 and 5,073,627,each of which is incorporated herein by reference. A preferred fusionprotein is PIXY321 as described in U.S. Pat. No. 5,199,942.

In addition to their use in ex vivo culture of dendritic cells,cytokines will also be useful in the present invention by separate,sequential or simultaneous administration of a cytokine or cytokineswith activated, antigen-pulsed dendritic cells. Preferred cytokines arethose that modulate an immune response, particularly cytokines selectedfrom the group consisting of Interleukins 1, 2, 3, 4, 5, 6, 7, 10, 12and 15; granulocyte-macrophage colony stimulating factor, granulocytecolony stimulating factor; a fusion protein comprising Interleukin-3 andgranulocyte-macrophage colony stimulating factor; Interferon-γ; TNF;TGF-β; flt-3 ligand; soluble CD40 ligand; biologically activederivatives of these cytokines; and combinations thereof. Soluble CD83,described in U.S. Ser. No. 08/601,954, filed Feb. 15, 1996), and solubleCD40L (described in U.S. Ser. No. 08/477,733 and U.S. Ser. No.08/484,624, both filed Jun. 7, 1995) are particularly preferredcytokines.

Useful cytokines act by binding a receptor present on the surface of adendritic cell and transducing a signal. Moreover, additional bindingproteins can be prepared as described herein for CD40 binding proteins,that bind appropriate cytokine receptors and transduce a signal to adendritic cell. For example, WO 95/27062 describes agonistic antibodiesto Flt-3, the receptor for Flt-3L, from which various Flt-3 binding.proteins can be prepared. Additional useful cytokines includebiologically active analogs of cytokicines that are useful for culturingdendritic cells. Useful cytokine analogs have an amino acid sequencethat is substantially similar to the native cytokine, and arebiologically active capable of binding to their specific receptor andtransducing a biological signal. Such analogs can be prepared and testedby methods that are known in the art and as described herein.

CD40/CD40L

CD40 is a member of the tumor necrosis factor (TNF)/nerve growth factor(NGF) receptor family, which is defined by the presence of cysteine-richmotifs in the extracellular region (Smith et al., Science 248:1019,1990; Mallett and Barclay, Immunology Today 12:220; 1991). This familyincludes the lymphocyte antigen CD27, CD30 (an antigen found onHodgkin's lymphoma and Reed-Stemberg cells), two receptors for TNF, amurine protein referred to as 4-1BB, rat OX40 antigen, NGF receptor, andFas antigen. Human CD40 antigen (CD40) is a peptide of 277 amino acidshaving a molecular weight of 30,600 (Stamenkovic et al., EMBO J. 8:1403,1989).

Activated CD4⁺ T cells express high levels of a ligand for CD40 (CD40L).Human CD40L was cloned from peripheral blood T-cells as described inSpriggs et al., J. Exp. Med. 176:1543 (1992). The cloning of murineCD40L is described in Armitage et al., Nature 357:80 (1992). CD40L is atype II membrane polypeptide having an extracellular region at itsC-terminus, a transmembrane region and an intracellular region at itsN-terminus. CD40L biological activity is mediated by binding of theextracellular region of CD40L with CD40, and includes B cellproliferation and induction of antibody secretion (including IgEsecretion).

CD40L is believed to be important in feedback regulation of an immuneresponse. For example, a CD40⁺ antigen presenting cell will presentantigen to a T cell, which will then become activated and express CD40L.The CD40L will, in turn, further activate the antigen presenting cell,increasing its efficiency at antigen presentation, and upregulatingexpression of Class I and Class II MHC, CD80 and CD86 costimulatorymolecules, as well as various cytokines (Caux et al., J. Exp. Med.180:1263, 1994).

Useful forms of CD40L for the inventive methods as disclosed in U.S.Ser. No. 08/477,733 and U.S. Ser. No. 08/484,624, both filed Jun. 7,1995, and both of which are incorporated by reference herein. Suchuseful forms include soluble, oligomeric CD40 ligand comprising aCD40-binding peptide and an oligomer-forming peptide. The CD40-bindingpeptide is selected from the group consisting of:

(a) a peptide comprising amino acids 1 through 261, 35 through 261, 34through 25, 113 through 261, 113 through 225, 120 through 261, or 120through 225 of SEQ ID NO:2;

(b) fragments of a peptide according to (a) that bind CD40; and

(c) peptides encoded by DNA which hybridizes to a DNA that encodes apeptide of (a) or (b), under stringent conditions (hybridization in6×SSC at 63° C. overnight; washing in 3×SSC at 55° C.), and which bindto CD40, Useful oligomer-forming peptides are also disclosed in U.S.Ser. No. 08/477,733 and U.S. Ser. No. 08/484,624, and exemplified in SEQID NOs: 3 and 4 herein. CD40 polypeptides may exist as oligomers, suchas dimers or trimers. Oligomers are linked by disulfide bonds formedbetween cysteine residues on different CD40L polypeptides.Alternatively, one can link two soluble CD40L domains with aGly₄SerGly₅Ser linker sequence, or other linker sequence described inU.S. Pat. No. 5,073,627, which is incorporated by reference herein.CD40L polypeptides may also be created by fusion of the C terminal ofsoluble CD40L to the Fc region of IgG1. CD40L/Fc fusion proteins areallowed to assemble much like heavy chains of an antibody molecule toform divalent CD40L. If fusion proteins are made with both heavy andlight chains of an antibody, it is possible to form a CD40L oligomerwith as many as four CD40L extracellular regions.

A corresponding family of ligands exists for molecules in the TNFRfamily, and several of these are also expressed on activated T cells orother cells of the immune system. This family includes tumor necrosisfactor and lymphotoxin (TNF and LT, respectively; reviewed in Ware etal., Curr. Top. Microbiol. Immunol. 198:175, 1995), as well as CD27L(U.S. Ser. No. 08/106,507, filed Aug. 13, 1993), CD30L (U.S. Pat. No.5,480,981, issued Jan. 2, 1996), 4-1BBL (U.S. Ser. No. 08/236,918, filedMay 6, 1994), OX40L (U.S. Pat. No. 5,457,035, issued Oct. 10, 1995) andFas L (U.S. Ser. No. 08/571,579, filed Dec. 13, 1995). These ligands arealso known to be involved in modulation of an immune response, and arelikely to be useful to activate antigen-pulsed dendritic cells or otherantigen presenting cells that bear the corresponding receptor.

CD40 Monoclonal Antibodies and Additional CD40 Binding Proteins

Useful CD40 binding proteins are those that are capable of binding CD40and inhibiting binding of CD40 to CD40L, as determined by observing atleast about 90% inhibition of the binding of soluble CD40 to CD40L, andinclude monoclonal antibodies, CD40 ligand, and molecules derivedtherefrom. Monoclonal antibodies directed against the CD40 surfaceantigen (CD40 mAb) have been shown to mediate various biologicalactivities on human B cells (see for example, Leukocyte Typing IV; A. J.McMichael ed. Oxford University Press. Oxford, p. 426). U.S. Ser. No.08/130, 541, filed Oct. 1, 1993, the relevant disclosure of which isincorporated by reference, discloses two monoclonal antibodies thatspecifically bind CD40, referred to as hCD40m2 and hCD40m3. Unlike otherCD40 mAb, hCD40m2 (ATCC HB 11459; deposited under terms of the BudapestTreaty with the American Type Culture Collection in Rockville, Md., USA,on Oct. 6, 1993) and hCD40m3 bind CD40 and inhibit binding of CD40 tocells that constitutively express CD40L, indicating that hCD40m2 andhCD40m3 bind CD40 in or near the ligand binding domain.

Additional CD40 monoclonal antibodies may be generated usingconventional techniques (see U.S. Pat. Nos. RE 32,011, 4,902,614,4,543,439, and 4,411,993 which are incorporated herein by reference; seealso Monoclonal Antibodies, Hybridomas: A New Dimension in BiologicalAnalyses, Plenum Press, Kennett, McKearn, and Bechtol (eds.), 1980, andAntibodies: A Laboratory Manual, Harlow and Lane (eds.), Cold SpringHarbor Laboratory Press, 1988, which are also incorporated herein byreference). Monoclonal antibodies that bind CD40 in or near the ligandbinding domain will also be useful in the present invention.

Additional CD40 binding proteins may also be constructed utilizingrecombinant DNA techniques. For example, the variable regions of a genewhich encodes an antibody to CD40 that binds in or near the ligandbinding domain can be incorporated into a useful CD40 binding protein(see Larrick et al., Biotechnology 7:934, 1989; Reichmann et al., Nature332:323, 1988; Roberts et al., Nature 328:731, 1987; Verhoeyen et al.,Science 239:1534, 1988; Chaudhary et al., Nature 339:394, 1989).

Briefly, DNA encoding the antigen-binding site (or CD40 binding domain;variable region) of a CD40 mAb is isolated, amplified, and linked to DNAencoding another protein, for example a human IgG (see Verhoeyen et al.,supra; see also Reichmann et al., supra). Alternatively, theantigen-binding site (variable region) may be either linked to, orinserted into, another completely different protein (see Chaudhary etal., supra), resulting in a new protein with antigen-binding sites ofthe antibody as well as the functional activity of the completelydifferent protein.

Similarly, the CD40 binding region (extracellular domain) of a CD40ligand may be used to prepare other CD40 binding proteins. Useful formsof CD40 ligand are disclosed in U.S. Ser. No.08/477,733 and U.S. Ser.No.08/484,624, both of which were filed on Jun. 7, 1995. Additionalforms of CD40 ligand can be prepared by methods known in the art. As forother useful CD40 binding proteins, CD40 ligand will bind CD40 in ornear the ligand binding domain, and will be capable of transducing asignal to a cell expressing CD40 (i.e., biologically active).

DNA sequences that encode proteins or peptides that form oligomers willbe particularly useful in preparation of CD40 binding proteinscomprising an antigen binding domain of CD40 antibody, or anextracellular domain of a CD40 ligand. Certain of such oligomer-formingproteins are disclosed in U.S. Ser. No.08/477,733 and U.S. Ser. No.08/484,624, both of which were filed on Jun. 7, 1995; additional, usefuloligomer-forming proteins are also disclosed in U.S. Ser. No.08/446,922,filed May 18, 1995. Fc fusion proteins (including those that are formedwith Fc muteins have decreased affinity for Fc receptors) can also beprepared.

Mutant forms of CD40 binding proteins that are substantially similar(i.e., those having an amino acid sequence at least 80% identical to anative amino acid sequence, most preferably at least 90% identical) tothe previously described CD40 binding proteins will also be useful inthe present invention. The percent identity may be determined, forexample, by comparing sequence information using the GAP computerprogram, version 6.0 described by Devereux et al. (Nucl. Acids Res.12:387, 1984) and available from the University of Wisconsin GeneticsComputer Group (UWGCG). The GAP program utilizes the alignment method ofNeedleman and Wunsch (J. Mol. Biol. 48:443, 1970), as revised by Smithand Waterman (Adv. Appi. Math 2:482, 1981). The preferred defaultparameters for the GAP program include: (1) a unary comparison matrix(containing a value of 1 for identities and 0 for non-identities) fornucleotides, and the weighted comparison matrix of Gribskov and Burgess,Nucl. Acids Res. 14:6745, 1986, as described by Schwartz and Dayhoff,eds., Atlas of Protein Sequence and Structure, National BiomedicalResearch Foundation, pp. 353-358, 1979; (2) a penalty of 3.0 for eachgap and an additional 0.10 penalty for each symbol in each gap; and (3)no penalty for end gaps.

Generally, substitutions of different amino acids from those in thenative form of a useful CD40 binding protein should be madeconservatively; i.e., the most preferred substitute amino acids arethose which do not affect the ability of the inventive proteins to bindCD40 in a manner substantially equivalent to that of native CD40 ligand.Examples of conservative substitutions include substitution of aminoacids outside of the binding domain(s), and substitution of amino acidsthat do not alter the secondary and/or tertiary structure of CD40binding proteins. Additional examples include substituting one aliphaticresidue for another, such as Ile, Val, Leu, or Ala for one another, orsubstitutions of one polar residue for another, such as between Lys andArg; Glu and Asp; or Gln and Asn. Other such conservative substitutions,for example, substitutions of entire regions having similarhydrophobicity characteristics, are well known.

Similarly, when a deletion or insertion strategy is adopted, thepotential effect of the deletion or insertion on biological activityshould be considered. Subunits of CD40 binding proteins may beconstructed by deleting terminal or internal residues or sequences.Additional guidance as to the types of mutations that can be made isprovided by a comparison of the sequence of CD40 binding proteins toproteins that have similar structures

Mutations must, of course, preserve the reading frame phase of thecoding sequences and preferably will not create complementary regionsthat could hybridize to produce secondary mRNA structures such as loopsor hairpins which would adversely affect translation of the CD40 bindingprotein mRNA. Although a mutation site may be predetermined, it is notnecessary that the nature of the mutation per se be predetermined. Forexample, in order to select for optimum characteristics of mutants at agiven site, random mutagenesis may be conducted at the target codon andthe expressed mutated proteins screened for the desired activity.

Mutations can be introduced at particular loci by synthesizingoligonucleotides containing a mutant sequence, flanked by restrictionsites enabling ligation to fragments of the native sequence. Followingligation, the resulting reconstructed sequence encodes an analog havingthe desired amino acid insertion, substitution, or deletion.Alternatively, oligonucleotide-directed site-specific mutagenesisprocedures can be employed to provide an altered gene having particularcodons altered according to the substitution, deletion, or insertionrequired. Exemplary methods of making the alterations set forth aboveare disclosed by Walder et al. (Gene 42:133, 1986); Bauer et al. (Gene37:73, 1985); Craik (BioTechniques, January 1985, 12-19); Smith et al.(Genetic Engineering: Principles and Methods, Plenum Press, 1981); andU.S. Pat. Nos. 4,518,584 and 4,737,462 disclose suitable techniques, andare incorporated by reference herein.

As is well-known in the art, not all mutations will cause a change inamino acid sequence. Mutations that confer advantageous properties inthe production of recombinant proteins will also be useful for preparinguseful CD40 binding proteins. Naturally occurring variants are alsoencompassed by the invention. Examples of such variants are proteinsthat result from alternate mRNA splicing events or from proteolyticcleavage of the protein, wherein the native biological property isretained.

Once suitable antibodies or binding proteins have been obtained, theymay be isolated or purified by many techniques well known to those ofordinary skill in the art (see Antibodies: A Laboratory Manual, Harlowand Lane (eds.), Cold Spring Harbor Laboratory Press, 1988). Suitabletechniques include peptide or protein affinity columns, HPLC or RP-HPLC,purification on protein A or protein G columns, or any combination ofthese techniques. Recombinant CD40 binding proteins can be preparedaccording to standard methods, and tested for binding specificity toCD40 utilizing assays known in the art, including for example ELISA,ABC, or dot blot assays, as well by bioactivity assays. The latter willalso be useful in evaluating the biological activity of CD40 bindingproteins.

Preparation of Antigens

Immunization is a centuries old, and highly effective, means of inducinga protective immune response against pathogens in order to prevent orameliorate disease. The vaccines that have been used for such inductionare generally live, attenuated microorganisms, or preparations of killedorganisms or fractions thereof. Live, attenuated vaccines are generallythought to more closely mimic the immune response that occurs with anatural infection than do those prepared from killed microbes ornon-infective preparations derived from pathogens (i.e., toxoids,recombinant protein vaccines). However, attenuated vaccines also presenta risk of reversion to pathogenicity, and can cause illness, especiallyin immunocompromised individuals.

Along with improved sanitation, immunization has been the most efficientmeans of preventing death or disability from numerous infectiousdiseases in humans and in other animals. Vaccination of susceptiblepopulations has been responsible for eliminating small pox world wide,and for drastic decreases in the occurrence of such diseases asdiphtheria, pertussis, and paralytic polio in the developed nations.Numerous vaccines are licensed for administration to humans, includinglive virus vaccines for certain adenoviruses, measles, mumps and rubellaviruses, and poliovirus, diphtheria and tetanus toxoid vaccines, andHaemophilus b and meningococcal polysaccharide vaccines (Hinman et al.,in Principles and Practice of Infectious Diseases, 3rd edition; G. L.Mandell, R. G. Douglas and J. E. Bennett, eds., Churchill LivingstoneInc., NY, N.Y.; 2320-2333; Table 2).

In addition to use in the area of infectious disease, vaccination isalso considered a promising therapy for cancer. For such uses,tumor-associated antioens can be prepared from tumor cells, either bypreparing crude lysates of tumor cells, for example as described inCohen et al., Cancer Res. 54:1055 (1994) and Cohen et al., Eur. J.Immunol. 24:315 (1994), or by partially purifying the antigens (forexample, as described by Itoh et al., J. Immunol. 153:1202; 1994).Moreover, useful tumor antigens may be purified further, or evenexpressed recombinantly, to provide suitable antigen preparations. Anyother methods of identifying and isolating antigens against which animmune response would be beneficial in cancer will also find utility inthe inventive methods.

Purified dendritic cells are then pulsed with (exposed to) antigen, toallow them to take up the antigen in a manner suitable for presentationto other cells of the immune systems. Antigens are classically processedand presented through two pathways. Peptides derived from proteins inthe cytosolic compartment are presented in the context of Class I MHCmolecules, whereas peptides derived from proteins that are found in theendocytic pathway are presented in the context of Class II MHC. However,those of skill in the art recognize that there are exceptions; forexample, the response of CD8⁺ tumor specific T cells, which recognizeexogenous tumor antigens expressed on MHC Class I. A review ofMHC-dependent antigen processing and peptide presentation is found inGermain, R. N., Cell 76:287 (1994).

Numerous methods of pulsing dendritic cells with antigen are known;those of skill in the art regard development of suitable methods for aselected antigen as routine experimentation. In general, the antigen isadded to cultured dendritic cells under conditions promoting viabilityof the cells, and the cells are then allowed sufficient time to take upand process the antigen, and express antigen peptides on the cellsurface in association with either Class I or Class II MHC, a period ofabout 24 hours (from about 18 to about 30 hours, preferably 24 hours).Dendritic cells may also be exposed to antigen by transfecting them withDNA encoding the antigen. The DNA is expressed, and the antigen ispresumably processed via the cytosolic/Class I pathway.

Administration of Activated Antigen-pulsed Dendritic Cells

The present invention provides methods of using therapeutic compositionscomprising activated, antigen-pulsed dendritic cells. The use of suchcells in conjunction with soluble cytolcine receptors or cytokines, orother immunoregulatory molecules is also contemplated. The inventivecompositions are administered to stimulate an immune response, and canbe given by bolus injection, continuous infusion, sustained release fromimplants, or other suitable technique. Typically, the cells on theinventive methods will be administered in the form of a compositioncomprising the antigen-pulsed, activated dendritic cells in conjunctionwith physiologically acceptable carriers, excipients or diluents. Suchcarriers will be nontoxic to recipients at the dosages andconcentrations employed. Neutral buffered saline or saline mixed withconspecific serum albumin are exemplary appropriate diluents.

For use in stimulating a certain type of immune response, administrationof other cytokines along with activated, antigen-pulsed dendritic cellsis also contemplated. Several useful cytokines (or peptide regulatoryfactors) are discussed in Schrader, J. W. (Mol Immunol 28:295; 1991).Such factors include (alone or in combination) Interleukins 1, 2, 4, 5,6, 7, 10, 12 and 15; granulocyte-macrophage colony stimulating factor,granulocyte colony stimulating factor; a fusion protein comprisingInterleukin-3 and granulocyte-macrophage colony stimulating factor;Interferon-γ, TNF, TGF-β, flt-3 ligand and biologically activederivatives thereof. A particularly preferred cytokine is CD40 ligand(CD40L). A soluble form of CD40L is described in U.S. Ser. No.08/484,624, filed Jun. 7, 1995. Other cytokines will also be useful, asdescribed herein. DNA encoding such cytokines will also be useful in theinventive methods, for example, by transfecting the dendritic cells toexpress the cytokines. Administration of these immunomodulatorymolecules includes simultaneous, separate or sequential administrationwith the cells of the present invention.

The relevant disclosures of all publications cited herein arespecifically incorporated by reference. The following examples areprovided to illustrate particular embodiments and not to limit the scopeof the invention.

EXAMPLE 1

This Example describes a method for generating purified dendritic cellsex vivo. Human bone marrow is obtained, and cells having a CD34⁺phenotype are isolated using a CD34 antibody column (CellPro, Bothell,Wash.). The CD34⁺ cells are cultured in a suitable medium, for example,McCoy's enhanced media, that contains cytokines that promote the growthof dendritic cells (i.e., 20 ng/ml each of GM-CSF, IL-4, TNF-α, or 100ng/ml flt3-L or c-kit ligand, or combinations thereof). The culture iscontinued for approximately two weeks at 37 ° C. in 10% CO₂ in humidair. Cells then are sorted by flow cytometry using antibodies for CD1a⁺,HLA-DR⁺ and CD86⁺. A combination of GM-CSF, L-4 and TNF-α can yield asix to seven-fold increase in the number of cells obtained after twoweeks of culture, of which 50-80% of cells are CD1a⁺HLA-DR⁺CD86⁺. Theaddition of flt3-L and/or c-kit ligand further enhances the expansion oftotal cells, and therefore of the dendritic cells. Phenotypic analysisof cells isolated and cultured under these conditions indicates thatbetween 60-70% of the cells are HLA-DR⁺, CD86⁺, with 40-50% of the cellsexpressing CD1a in all factor combinations examined.

EXAMPLE 2

This Example describes a method for collecting and expanding dendriticcells. Prior to cell collection, flt3-L or sargramostim (Leukine®,Immunex Corporation, Seattle, Wash.) may be administered to anindividual to mobilize or increase the numbers of circulating PBPC andPBSC. Other growth factors such as CSF-1, GM-CSF, c-kit ligand, G-CSF,EPO, IL-1, IL-2, IL-3, IL-4, IL-5, IL-6, IL-7, IL-8, IL-9, IL-10, IL-11,IL-12, IL-13, IL-14, IL-15, GM-CSF/IL-3 fusion proteins, LIF, FGF andcombinations thereof, can be likewise administered in sequence, or inconcurrent combination with flt3-L.

Mobilized or non-mobilized PBPC and PBSC are collected using apheresisprocedures known in the art. See, for example, Bishop et al., Blood,vol. 83, No. 2, pp. 610-616 (1994). Briefly, PBPC and PBSC are collectedusing conventional devices, for example, a Haemonetics Model V50apheresis device (Haemonetics, Braintree, Mass.). Four-hour collectionsare performed typically no more than five times weekly untilapproximately 6.5×10⁸ mononuclear cells (MNC)/kg individual arecollected.

Aliquots of collected PBPC and PBSC are assayed forgranulocyte-macrophage colony-forming unit (CFU-GM) content. Briefly,MNC (approximately 300,000) are isolated, cultured at 37° C. in 5% CO₂in fully humidified air for about two weeks in modified McCoy's 5Amedium, 0.3% acar, 200 U/ml recombinant human GM-CSF, 200 u/mirecombinant human IL-3, and 200 u/ml recombinant human G-CSF. Othercytokines, including flt3-L or GM-CSF/IL-3 fusion molecules (PIXY 321),may be added to the cultures. These cultures are stained with Wright'sstain, and CFU-GM colonies are scored using a dissecting microscope(Ward et al., Exp. Hematol., 16:358 (1988). Alternatively, CFU-GMcolonies can be assayed using the CD34/CD33 flow cytometry method ofSiena et al., Blood, Vol. 77, No. 2, pp 400-409 (1991), or any othermethod known in the art.

CFU-GM containing cultures are frozen in a controlled rate freezer(e.g., Cryo-Med, Mt. Clemens, Mich.), then stored in the vapor phase ofliquid nitrogen. Ten percent dimethylsulfoxide can be used as acryoprotectant. After all collections from the individual have beenmade, CFU-GM containing cultures are thawed and pooled, then contactedwith flt3-L either alone, sequentially or in concurrent combination withother cytokines listed above to drive the CFU-GM to dendritic celllineage. The dendritic cells are cultured and analyzed for percentage ofcells displaying selected markers as described above.

EXAMPLE 3

This example illustrates the ability of CD40L-stimulated dendritic cellsto present allo-antigen and therefore cause proliferation of T cells.CD34⁺ cells were obtained from the bone marrow of a human donor,cultured for two weeks in the presence of selected cytokines, andisolated by flow cytometry substantially as described in Example 1.Prior to their use in a mixed lymphocyte reaction (MLR), the dendriticcells were cultured for an additional 24 hours in the presence orabsence of a soluble trimeric form of CD40L (1 μg/ml) in McCoy'senhanced media containing cytokines that support the growth of dendriticcells.

T cells were purified from the blood of a non-HLA matched donor byrosetting with 2-arninoethylisothiouronium bromide hydrobromide-treatedsheep red blood cells. CD4⁺ and CD8⁺ populations were further purifiedusing immunomagnetic selection using a MACS (Milenyi Biotec, Sunnyvale,Calif.) according to the manufacturer's protocol. Cell proliferationassays were conducted with the purified T cells in RPMI (10%heat-inactivated fetal bovine serum (FBS)), in the presence of titratednumbers of the dendritic cells, at 37° C. in a 10% CO₂ atmosphere.Approximately 1×10⁵ T cells per well were cultured in triplicate inround-bottomed 96-well microtiter plates (Corning) for seven days, inthe presence of varying numbers of the unmatched dendritic cells. Thecells were pulsed with 1 μCi/well of tritiated thymidine (25 Ci/nmole,Amershain, Arlington Heights, Ill.) for the final eight hours ofculture.

Cells were harvested onto glass fiber discs with an automated cellharvester and incorporated cpm were measured by liquid scintillationspectrometry. The results, which are shown in FIG. 1, demonstrated thatthree-fold fewer CD40L-activated dendritic cells were required tostimulate the equivalent proliferation of T cells compared to dendriticcells that had not been exposed to CD40L prior to their use in an MLR.This increase was most likely due to increased expression of cellsurface molecules that stimulate allo-reactive T cells.

EXAMPLE 4

This example illustrates the ability of dendritic cells to stimulateantigen-specific proliferation of T cells. CD34⁺ cells were obtainedfrom the bone marrow of a human donor believed to be reactive againsttetanus toxoid, cultured for two weeks in the presence of selectedcytokines, and isolated by flow cytometry substantially as described inExample 1. Prior to their use in a tetanus toxid (TTX) antigenpresentation assay, the dendritic cells were cultured for an additional24 hours in the presence or absence of a soluble trimeric form of CD40L(1 μg/ml) in McCoy's enhanced media containing cytokines that supportthe growth of dendritic cells, then pulsed with purified TTX (ConnaughtLaboratory Inc., Swiftwater, Pa.), at 37° C. in a 10% CO₂ atmosphere for24 hrs.

Autologous tetanus toxoid-reactive T cells were derived by culturing theCD34⁻ cells that were eluted from the CD34 antibody column in thepresence of purified TTX and low concentrations of IL-2 and IL-7 (2ng/ml and 5 ng/ml, respectively) for two weeks. The CD34⁻ populationcontains a percentage of T cells (about 5%), a proportion of which arcreactive against tetanus toxoid, as well as other cell types that act asantigen presenting cells. By week 2, analysis of these cells indicatedthat they were about 90% T cells, the majority of which were tetanustoxoid-specific, with low levels of the T cell activation markers.

Antigen specific T cell proliferation assays were conducted withTTX-specific T cells from CD34⁻ bone marrow cells as above, in RPMI withadded 10% heat-inactivated fetal bovine serum (FBS), in the presence ofthe tetanus toxoid-pulsed dendritic cells, at 37° C. in a 10% CO₂atmosphere. Approximately 1×10⁵ T cells per well were cultured intriplicate in round-bottomed 96-well microtiter plates (Corning) forfive days, in the presence of a titrated number of dendritic cells. Thecells were pulsed with 1 μCi/well of tritiated thymnidine (25 Ci/nmole,Amersham, Arlington Heights, Ill.) for the final four to eight hours ofculture. Cells were harvested onto glass fiber discs with an automatedcell harvester and incorporated cpm were measured by liquidscintillation spectrometry. The results, which are shown in FIG. 2,indicated that dendritic cells that are cultured with CD40L are aboutten-fold less efficient at presenting antigen to TTX-specific T cellsthan dendritic cells that were not exposed to CD40L.

EXAMPLE 5

This example illustrates the ability of CD40L to activate antigen-pulseddendritic cells for stimulation of antigen-specific T cells. CD34⁺ cellswere obtained and treated as described in Example 4, except that thecells were pulsed with tetanus toxoid for 24 hours prior to culture withCD40L. Autologous tetanus toxoid-reactive T cells were derived, andantigen specific T cell proliferation assays conducted, as described inExample 4. The results, which are shown in FIG. 3, indicated thatthree-fold fewer dendritic cells that are first pulsed with antigen,then cultured with CD40L, were required to stimulate the equivalentlevel of proliferation when presenting TTX to TTX-specific T cells thandendritic cells that were pulsed with antigen but not exposed to CD40L.

4 840 base pairs nucleic acid single linear cDNA NO NO Homo sapiensCD40-L CDS 46..831 1 TGCCACCTTC TCTGCCAGAA GATACCATTT CAACTTTAAC ACAGCATG ATC GAA 54 Met Ile Glu 1 ACA TAC AAC CAA ACT TCT CCC CGA TCT GCG GCCACT GGA CTG CCC ATC 102 Thr Tyr Asn Gln Thr Ser Pro Arg Ser Ala Ala ThrGly Leu Pro Ile 5 10 15 AGC ATG AAA ATT TTT ATG TAT TTA CTT ACT GTT TTTCTT ATC ACC CAG 150 Ser Met Lys Ile Phe Met Tyr Leu Leu Thr Val Phe LeuIle Thr Gln 20 25 30 35 ATG ATT GGG TCA GCA CTT TTT GCT GTG TAT CTT CATAGA AGG TTG GAC 198 Met Ile Gly Ser Ala Leu Phe Ala Val Tyr Leu His ArgArg Leu Asp 40 45 50 AAG ATA GAA GAT GAA AGG AAT CTT CAT GAA GAT TTT GTATTC ATG AAA 246 Lys Ile Glu Asp Glu Arg Asn Leu His Glu Asp Phe Val PheMet Lys 55 60 65 ACG ATA CAG AGA TGC AAC ACA GGA GAA AGA TCC TTA TCC TTACTG AAC 294 Thr Ile Gln Arg Cys Asn Thr Gly Glu Arg Ser Leu Ser Leu LeuAsn 70 75 80 TGT GAG GAG ATT AAA AGC CAG TTT GAA GGC TTT GTG AAG GAT ATAATG 342 Cys Glu Glu Ile Lys Ser Gln Phe Glu Gly Phe Val Lys Asp Ile Met85 90 95 TTA AAC AAA GAG GAG ACG AAG AAA GAA AAC AGC TTT GAA ATG CAA AAA390 Leu Asn Lys Glu Glu Thr Lys Lys Glu Asn Ser Phe Glu Met Gln Lys 100105 110 115 GGT GAT CAG AAT CCT CAA ATT GCG GCA CAT GTC ATA AGT GAG GCCAGC 438 Gly Asp Gln Asn Pro Gln Ile Ala Ala His Val Ile Ser Glu Ala Ser120 125 130 AGT AAA ACA ACA TCT GTG TTA CAG TGG GCT GAA AAA GGA TAC TACACC 486 Ser Lys Thr Thr Ser Val Leu Gln Trp Ala Glu Lys Gly Tyr Tyr Thr135 140 145 ATG AGC AAC AAC TTG GTA ACC CTG GAA AAT GGG AAA CAG CTG ACCGTT 534 Met Ser Asn Asn Leu Val Thr Leu Glu Asn Gly Lys Gln Leu Thr Val150 155 160 AAA AGA CAA GGA CTC TAT TAT ATC TAT GCC CAA GTC ACC TTC TGTTCC 582 Lys Arg Gln Gly Leu Tyr Tyr Ile Tyr Ala Gln Val Thr Phe Cys Ser165 170 175 AAT CGG GAA GCT TCG AGT CAA GCT CCA TTT ATA GCC AGC CTC TGCCTA 630 Asn Arg Glu Ala Ser Ser Gln Ala Pro Phe Ile Ala Ser Leu Cys Leu180 185 190 195 AAG TCC CCC GGT AGA TTC GAG AGA ATC TTA CTC AGA GCT GCAAAT ACC 678 Lys Ser Pro Gly Arg Phe Glu Arg Ile Leu Leu Arg Ala Ala AsnThr 200 205 210 CAC AGT TCC GCC AAA CCT TGC GGG CAA CAA TCC ATT CAC TTGGGA GGA 726 His Ser Ser Ala Lys Pro Cys Gly Gln Gln Ser Ile His Leu GlyGly 215 220 225 GTA TTT GAA TTG CAA CCA GGT GCT TCG GTG TTT GTC AAT GTGACT GAT 774 Val Phe Glu Leu Gln Pro Gly Ala Ser Val Phe Val Asn Val ThrAsp 230 235 240 CCA AGC CAA GTG AGC CAT GGC ACT GGC TTC ACG TCC TTT GGCTTA CTC 822 Pro Ser Gln Val Ser His Gly Thr Gly Phe Thr Ser Phe Gly LeuLeu 245 250 255 AAA CTC TGAACAGTGT CA 840 Lys Leu 260 261 amino acidsamino acid linear protein 2 Met Ile Glu Thr Tyr Asn Gln Thr Ser Pro ArgSer Ala Ala Thr Gly 1 5 10 15 Leu Pro Ile Ser Met Lys Ile Phe Met TyrLeu Leu Thr Val Phe Leu 20 25 30 Ile Thr Gln Met Ile Gly Ser Ala Leu PheAla Val Tyr Leu His Arg 35 40 45 Arg Leu Asp Lys Ile Glu Asp Glu Arg AsnLeu His Glu Asp Phe Val 50 55 60 Phe Met Lys Thr Ile Gln Arg Cys Asn ThrGly Glu Arg Ser Leu Ser 65 70 75 80 Leu Leu Asn Cys Glu Glu Ile Lys SerGln Phe Glu Gly Phe Val Lys 85 90 95 Asp Ile Met Leu Asn Lys Glu Glu ThrLys Lys Glu Asn Ser Phe Glu 100 105 110 Met Gln Lys Gly Asp Gln Asn ProGln Ile Ala Ala His Val Ile Ser 115 120 125 Glu Ala Ser Ser Lys Thr ThrSer Val Leu Gln Trp Ala Glu Lys Gly 130 135 140 Tyr Tyr Thr Met Ser AsnAsn Leu Val Thr Leu Glu Asn Gly Lys Gln 145 150 155 160 Leu Thr Val LysArg Gln Gly Leu Tyr Tyr Ile Tyr Ala Gln Val Thr 165 170 175 Phe Cys SerAsn Arg Glu Ala Ser Ser Gln Ala Pro Phe Ile Ala Ser 180 185 190 Leu CysLeu Lys Ser Pro Gly Arg Phe Glu Arg Ile Leu Leu Arg Ala 195 200 205 AlaAsn Thr His Ser Ser Ala Lys Pro Cys Gly Gln Gln Ser Ile His 210 215 220Leu Gly Gly Val Phe Glu Leu Gln Pro Gly Ala Ser Val Phe Val Asn 225 230235 240 Val Thr Asp Pro Ser Gln Val Ser His Gly Thr Gly Phe Thr Ser Phe245 250 255 Gly Leu Leu Lys Leu 260 740 base pairs nucleic acid singlelinear cDNA NO NO HUMAN IgG1 Fc 3 CGGTACCGCT AGCGTCGACA GGCCTAGGATATCGATACGT AGAGCCCAGA TCTTGTGACA 60 AAACTCACAC ATGCCCACCG TGCCCAGCACCTGAACTCCT GGGGGGACCG TCAGTCTTCC 120 TCTTCCCCCC AAAACCCAAG GACACCCTCATGATCTCCCG GACCCCTGAG GTCACATGCG 180 TGGTGGTGGA CGTGAGCCAC GAAGACCCTGAGGTCAAGTT CAACTGGTAC GTGGACGGCG 240 TGGAGGTGCA TAATGCCAAG ACAAAGCCGCGGGAGGAGCA GTACAACAGC ACGTACCGGG 300 TGGTCAGCGT CCTCACCGTC CTGCACCAGGACTGGCTGAA TGGCAAGGAC TACAAGTGCA 360 AGGTCTCCAA CAAAGCCCTC CCAGCCCCCATGCAGAAAAC CATCTCCAAA GCCAAAGGGC 420 AGCCCCGAGA ACCACAGGTG TACACCCTGCCCCCATCCCG GGATGAGCTG ACCAAGAACC 480 AGGTCAGCCT GACCTGCCTG GTCAAAGGCTTCTATCCCAG GCACATCGCC GTGGAGTGGG 540 AGAGCAATGG GCAGCCGGAG AACAACTACAAGACCACGCC TCCCGTGCTG GACTCCGACG 600 GCTCCTTCTT CCTCTACAGC AAGCTCACCGTGGACAAGAG CAGGTGGCAG CAGGGGAACG 660 TCTTCTCATG CTCCGTGATG CATGAGGCTCTGCACAACCA CTACACGCAG AAGAGCCTCT 720 CCCTGTCTCC GGGTAAATGA 740 33 aminoacids amino acid linear peptide 4 Arg Met Lys Gln Ile Glu Asp Lys IleGlu Glu Ile Leu Ser Lys Il 1 5 10 15 Tyr His Ile Glu Asn Glu Ile Ala ArgIle Lys Lys Leu Ile Gly Gl 20 25 30 Arg

What is claimed is:
 1. A method of stimulating an immune response in anindividual, comprising the steps of: (a) obtaining dendritic cells fromthe individual; (b) exposing the dendritic cells to an antigen inculture under conditions promoting uptake and processing of the antigento provide antigen-expressing dendritic cells; (c) contacting theantigen-expressing dendritic cells with a polypeptide selected from thegroup consisting of oligomeric CD40L and an antibody to CD40 to provideactivated antigen-expressing dendritic cells, wherein the antibody toCD40 transduces a signal to a cell expressing CD40; (d) administeringthe activated, antigen-expressing dendritic cells to the individual. 2.The method according to claim 1, wherein the dendritic cells areobtained by obtaining hematopoietic stem or progenitor cells from theindividual, and contacting the hematopoietic stem or progenitor cellswith a molecule selected from the group consisting of flt-3 ligand,GM-CSF, IL-4, TNF-α, IL-3, c-kit ligand, fusions of GM-CSF and IL-3, andcombinations thereof.
 3. The method according to claim 1, wherein theoligomeric CD40L comprises a soluble CD40L selected from the groupconsisting of: (a) a peptide comprising amino acids 1 through 261, 35through 261, 34 through 225, 113 through 261, 113 through 225, 120through 261, or 120 through 225 of SEQ ID NO:2; (b) fragments of apeptide according to (a) that bind CD40; and (c) peptides encoded by DNAwhich hybridizes to a DNA that encodes a peptide of (a) or (b), understringent conditions (hybridization in 6×SSC at 63° C. overnight;washing in 3×SSC at 55° C.), and which bind to CD40.
 4. The methodaccording to claim 3, wherein the soluble, oligomeric CD40L is selectedfrom the group consisting of: (a) a polypeptide having an amino acidsequence as set forth in SEQ ID NO:2 wherein a cysteine at amino acid194 is replaced with another amino acid; and (b) a polypeptide that is afragment of the polypeptide (a) that binds CD40; wherein the amino acidthat is substituted for the cysteine at amino acid 194 is selected fromthe group consisting of tryptophan, serine, aspartic acid, and lysine.5. The method according to claim 1, wherein flt-3 ligand is administeredto the individual prior to obtaining the dendritic cells, to expand thenumber of progenitor cells in the circulation of the individual.
 6. Themethod according to claim 5, wherein the dendritic cells are obtained byobtaining hematopoietic stem or progenitor cells from the individual,and contacting the hematopoietic stem or progenitor cells with amolecule selected from the group consisting of flt-3 ligand, GM-CSF,IL-4, TNF-α, IL-3, c-kit ligand, fusions of GM-CSF and IL-3, andcombinations thereof.
 7. The method according to claim 1, wherein theantigen-expressing, activated dendritic cells are administeredsimultaneously, sequentially or separately with a molecule selected fromthe group consisting of Interleukin (IL)-1, IL-2, IL-3, IL-4, IL-5,IL-6, IL-7, IL-10, IL-12, IL-15, granulocyte-macrophage colonystimulating factor, granulocyte colony stimulating factor, a fusionprotein comprising Interleukin-3 and granulocyte-macrophage colonystimulating factor, Interferon-γ, TNF, TGF-β, flt-3 ligand, soluble CD40ligand, and soluble CD83.
 8. The method according to claim 5, whereinthe oligomeric CD40L comprises a soluble CD40 ligand selected from thegroup consisting of: (a) a peptide comprising amino acids 1 through 261,35 through 261, 34 through 225, 113 through 261, 113 through 225, 120through 261, or 120 through 225 of SEQ ID NO:2; (b) fragments of apeptide according to (a) that bind CD40; (c) peptides encoded by DNAwhich hybridizes to a DNA that encodes a peptide of (a) or (b), understringent conditions (hybridization in 6×SSC at 63° C. overnight;washing in 3×SSC at 55° C.), and which bind to CD40; (d) a polypeptideaccording to (a) wherein the cysteine at amino acid 194 is replaced withanother amino acid selected from the group consisting of tryptophan,serine, aspartic acid, and lysine; and (e) a fragment of the polypeptideof (d) which binds CD40.
 9. The method according to claim 6, wherein theoligomeric CD40L comprises a soluble CD40 ligand selected from the groupconsisting of: (a) a peptide comprising amino acids 1 through 261, 35through 261, 34 through 225, 113 through 261, 113 through 225, 120through 261, or 120 through 225 of SEQ ID NO:2; (b) fragments of apeptide according to (a) that bind CD40; (c) peptides encoded by DNAwhich hybridizes to a DNA that encodes a peptide of (a) or (b), understringent conditions (hybridization in 6×SSC at 63° C. overnight;washing in 3×SSC at 55° C.), and which bind to CD40; (d) a polypeptideaccording to (a) wherein the a cysteine at amino acid 194 is replacedwith another amino acid selected from the group consisting oftryptophan, serine, aspartic acid, and lysine; and (e) a fragment of thepolypeptide of (d) which binds CD40.
 10. The method according to claim7, wherein the oligomeric CD40L comprises a soluble, CD40 ligandselected from the group consisting of: (a) a peptide comprising aminoacids 1 through 261, 35 through 261, 34 through 225, 113 through 261,113 through 225, 120 through 261, or 120 through 225 of SEQ ID NO:2; (b)fragments of a peptide according to (a) that bind CD40; (c) peptidesencoded by DNA which hybridizes to a DNA that encodes a peptide of (a)or (b), under stringent conditions (hybridization in 6×SSC at 63° C.overnight; washing in 3×SSC at 55° C.), and which bind to CD40; (d) apolypeptide according to (a) wherein the a cysteine at amino acid 194 isreplaced with another amino acid selected from the group consisting oftryptophan, serine, aspartic acid, and lysine; and (e) a fragment of thepolypeptide of (d) which binds CD40.
 11. A method for stimulating animmune response comprising the steps of: (a) obtaining hematopoieticstem or progenitor cells from an individual; (b) obtaining dendriticcells by contacting, in vitro, the cells of step (a) with cytokinessuitable for culturing dendritic cells; (c) exposing the dendritic cellsof step (b) to an antigen in vitro under conditions promoting uptake andprocessing of the vaccine so as to obtain antigen-expressing dendriticcells; (d) contacting the antigen-expressing dendritic cells with apolypeptide selected from the group consisting of oligomeric CD40L andan antibody to CD40, to provide activated antigen-expressing dendriticcells, wherein the antibody to CD40 transduces a signal to a cellexpressing CD40; and, (e) administering an effective amount of theactivated antigen-expressing dendritic cells of step (d) to theindividual.
 12. The method according to claim 11, wherein the oligomericCD40L comprises a polypeptide selected from the group consisting of: (a)a soluble, oligomeric CD40 ligand comprising amino acids 1-261 of SEQ IDNO:2 and an oligomer-forming peptide; (b) a soluble, oligomeric CD40ligand comprising amino acids 35-261 of SEQ ID NO:2 and anoligomer-forming peptide; (c) a soluble, oligomeric CD40 ligandcomprising amino acids 34-225 of SEQ ID NO:2 and an oligomer-formingpeptide; (d) a soluble, oligomeric CD40 ligand comprising amino acids113-261 of SEQ ID NO:2 and an oligomer-forming peptide; (e) a soluble,oligomeric CD40 ligand comprising amino acids 113-225 of SEQ ID NO:2 andan oligomer-forming peptide; (f) a soluble, oligomeric CD40 ligandcomprising amino acids 120-261 of SEQ ID NO:2 and an oligomer-formingpeptide; (g) a soluble, oligomeric CD40 ligand comprising amino acids120-225 of SEQ ID NO:2 and an oligomer-forming peptide; and fragments ofa polypeptide according to (a)-(g) that bind CD40.
 13. The method ofclaim 12 wherein the oligomer-forming peptide is an immunoglobulin heavychain encoded by nucleotides 1-740 of SEQ ID NO:3.
 14. The method ofclaim 12 wherein the oligomer-forming peptide is a leucine zipperrepresented by amino acids 1-33 of SEQ ID NO:4.
 15. The method of claim11 wherein the cysteine at amino acid 194 of SEQ ID NO:2 is substitutedwith an amino acid selected from the group consisting of tryptophan,serine, aspartic acid and lysine.